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Updated: Sep 27, 2025

Microdissection of Mouse Brain into Functionally and Anatomically Different Regions
Published on: February 15, 2021
Resolution and b value dependent structural connectome in ex vivo mouse brain.
Stephanie Crater1, Surendra Maharjan2, Yi Qi3
1Pratt School of Engineering, Duke University, Durham, North Carolina, USA.
High-resolution diffusion MRI (dMRI) in mouse brains reveals optimal parameters for structural connectome mapping. Achieving consistent tractography requires over 50 angles, while single-shell acquisitions with a b-value of 3000 s/mm² offer comparable results to multi-shell data.
Area of Science:
- Neuroimaging
- Biomedical Engineering
- Computational Neuroscience
Background:
- Diffusion MRI (dMRI) is crucial for mapping tissue microstructure and brain connectivity in clinical and preclinical research.
- Existing dMRI protocols, like those from the Human Connectome Project (HCP), are optimized for humans but less explored in preclinical rodent models.
- High-quality dMRI datasets are essential for accurate structural connectome reconstruction, particularly in small animal models like mice.
Purpose of the Study:
- To acquire and characterize high-quality, high-resolution dMRI datasets of ex vivo mouse brains using a 9.4T system.
- To systematically investigate the impact of key acquisition parameters (b-value, angular resolution, spatial resolution) on structural connectome outcomes.
- To provide guidelines for optimizing dMRI acquisition strategies in preclinical rodent studies.
Main Methods:
- Acquisition of dMRI datasets from mouse brains using a 9.4T MRI system from two vendors.
- Acquisition of a unique high-spatial resolution dataset (25 µm isotropic, 126 directions) and a high-angular resolution dataset (50 µm isotropic, 384 directions).
- Systematic investigation of b-values (1000–8000 s/mm²), angular resolution (10–126 directions), and spatial resolution (25–200 µm) effects on tractography and connectome metrics.
Main Results:
- Tractography stability and connectome accuracy significantly improve with angular resolution, with over 50 diffusion encoding directions being critical for consistent results.
- A linear relationship (R² > 0.99) was observed between connectome parameters and b-values, indicating that single-shell acquisitions at 3000 s/mm² can yield results comparable to multi-shell data.
- Decreased spatial resolution led to a lower Dice coefficient and increased false positive and false negative rates in connectome reconstruction.
Conclusions:
- This study establishes foundational guidelines for optimizing dMRI acquisition parameters in ex vivo mouse brains for structural connectome mapping.
- Trade-offs between spatial resolution, angular resolution, and b-value are critical for balancing data quality, acquisition time, and connectome accuracy.
- The findings support the development of efficient and effective dMRI protocols for preclinical neuroscience research.
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